Transport of dissolved organic carbon in streams of differing physiographic characteristics

Transport of dissolved organic carbon (DOC) in four river systems in different physiographic regions of the United States was related to link magnitude by a power function, log Y = ?0.84 + 1.24 log X. Multiple linear regression indicated that discharge, watershed area, and link magnitude explained almost all variation in DOC transport. For purposes of ecosystem comparison, link magnitude appeared superior to other classification systems, such as stream order.In two of the river systems, the largest fraction of DOC was transported in the spring. A third has a winter transport maximum; the last had bimodal spring and fall maxima.Streams transporting similar total amounts of DOC may vary widely in DOC concentration (mg. 1^?1). Particulate organic matter concentration was not simply related to that of DOC.Ranges and means of DOC concentration, mean DOC: POC ratios, annual load of transported DOC as well as annual watershed DOC output were tabulated for 45 streams and rivers, representing a broad range of stream systems and physiographic regions. Mean DOC concentration for these 45 waterways ranged from 0.7 to 28 mg. 1^?1. The very low DOC values are found in undisturbed streams; many of the higher values are associated with larger streams influenced by human activities. Most DOC outputs fell within the range 0.21–5.42 metric tons. km^?2.yr^?1; mean DOC:POC ranged between 0.09 and 70.A comparison was made among several biomes of the ratio of experted DOC to watershed gross and net primary production. DOC, while playing a major role in aquatic ecosystem organic budgets, appears to be of little significance in the nutrient balance of watersheds.     

Production of dissolved organic carbon in forest soils along the north–south European transect

The aim of this study is to estimate the C loss from forest soils due to the production of dissolved organic C (DOC) along a north–south European transect. Dissolved organic matter (DOM) was extracted from the forest soils incubated at a controlled temperature and water content. Soils were sampled from forest plots from Sweden to Italy. The plots represent monocultures of spruce, pine and beech and three selected chronosequences of spruce and beech spanning a range of mean annual temperature from 2 to 14 °C. The DOM was characterized by its DOC/DON ratio and the C isotope composition δ¹³C. The DOC/DON ratio of DOM varied from 25 to 15 after 16 days of incubation and it decreased to between 16 and 10 after 126 days. At the beginning of incubation the δ¹³C values of DOC were 1‰ or 2‰ less negative than incubated soils. At the end of the experiment δ¹³C of DOC were the same as soil values. In addition to DOC production heterotrophic respiration and N mineralization were measured on the incubated soils. The DON production rates decreased from 30 to 5 μgN gC⁻¹ d⁻¹ after 16 days of incubation to constant values from 5 to 2 μgN gC⁻¹ d⁻¹ after 126 days at the end of experiment. The DIN production rates were nearly constant during the experiments with values ranging from 20 to 4 μgN gC⁻¹ d⁻¹. DOC production followed first-order reaction kinetics and heterotrophic respiration followed zero-order reaction kinetics. Kinetic analysis of the experimental data yielded mean annual DOC and respiration productions with respect to sites. Mean annual estimates of DOC flux varied from 3 to 29 g of C m⁻² (1–19 mg C g⁻¹ of available C), corresponding to mean DOC concentrations from 2 to 85 mg C L⁻¹.     

Large-volume ultrafiltration for the study of radiocarbon signatures and size vs. age relationships in marine dissolved organic matter

In recent decades, tangential-flow ultrafiltration (UF) technology has become a primary tool for isolating large amounts of “ultrafiltered” marine dissolved organic carbon (UDOC; 0.1 μm to ∼1 nm) for the detailed characterization of DOC chemical composition and radiocarbon (Δ¹⁴C) signatures. However, while total DOC Δ¹⁴C values are generally thought to be quite similar in the world ocean, previous studies have reported widely different Δ¹⁴C values for UDOC, even from very similar ocean regions, raising questions about the relative “reactivity” of high molecular weight (HMW) DOC. Specifically, to what degree do variations in DOM molecular weight (MW) vs. composition alter its relative persistence, and therefore HMW DOC Δ¹⁴C values?In this study we evaluate the effects of varying proportions of HMW vs. low molecular weight (LMW) DOC on UDOC Δ¹⁴C values. Using concentration factor (CF) as a proxy for MW distributions, we modeled the retention of both OC and Δ¹⁴C in several very large CF experiments (CF >3000), from three depths (20, 670, and 915 m) in the North Pacific Subtropical Gyre (NPSG). The resulting DOC and Δ¹⁴C UF permeation coefficients generally increase with depth, consistent with mass balance trends, indicating very significant permeation of LMW, ¹⁴C-depleted DOC at depth, and higher recoveries of Δ¹⁴C-enriched, HMW DOC in the surface. In addition, changes in CF during sample concentration and ionic strength during sample diafiltration had very large and predictable impacts on UDOC Δ¹⁴C values.Together these results suggest that previously reported disparities in UDOC Δ¹⁴C values are reconciled by linked trends of Δ¹⁴C content vs. MW. At low CFs, UDOC samples have similar Δ¹⁴C values to total DOC. In contrast, UDOC samples collected at extremely high CFs (and after diafiltration) have more positive Δ¹⁴C values. We demonstrate that the observed relationships between UDOC Δ¹⁴C and CF derived from our data can directly explain offsets in all previously published UDOC Δ¹⁴C values for the NPSG. While CF is not traditionally considered in UF studies, our results indicate it can substantially influence the interpretation of UDOC ¹⁴C “age”, and thus reactivity, in the marine environment. In addition, our results indicate that CF can in fact be used as a proxy for average MW. We suggest that a variable-CF-UF approach, coupled with molecular-level Δ¹⁴C analyses, presents a new tool for studying relationships between molecular size, age, and “labile” DOC distributions in the ocean.     

Organic carbon concentrations and transport in small mountain rivers,Panama

Tropical small mountainous rivers (SMRs) are increasingly recognized for their role in the global export of dissolved organic carbon (DOC) to the oceans. Here we utilize the Isthmus of Panama as an ideal place to provide first-order estimates of DOC yields across a wide assemblage of bedrock lithologies and land cover practices. Samples for dissolved organic carbon (DOC) analysis were collected across Panama along an E–W transect from the central Panama area to the Costa Rican border for 24 mainstem rivers, 3 large tributary rivers, and one headwater stream. Sampling occurred during both the wet and the dry seasons. DOC concentrations during the wet season are higher than during the dry season in all but three of the rivers. Concentrations vary greatly from river to river and from season to season, with values as low as 0.64 mg l⁻¹ to greater than >25 mg l⁻¹ with the highest concentrations observed for the rivers draining Tertiary marine sedimentary rocks in the Burica and Azuero peninsulas. DOC yields from Panamanian rivers (2.29–7.97 tons/km²/y) are similar to or slightly lower than those determined for other tropical SMR systems. Areas underlain by Tertiary aged sediments exhibited significantly higher mean DOC yields compared to their igneous counterparts, despite maintaining substantially lower aboveground carbon densities, suggesting the important influence of lithology. Finally, regression analyses between DOC yields and select watershed parameters revealed a negative and statistically significant relationship with maximum and mean gradient suggesting lower soil retention times may be linked to lower DOC yields.     

Conservative behaviour of riverine dissolved organic carbon in the Severn Estuary: chemical and geochemical implications

The distribution, variability and chemical behaviour of dissolved organic carbon (DOC) was investigated over 2$\text{1}\text{2}$ years in the Severn Estuary and Bristol Channel, UK. The concentrations of riverine DOC (3.1–7.8 mg C l^?1) covaried with river flow and were invariably conservative in this turbid slowly flushing (~200 days) estuary, indicating that any microbial degradation, chemical flocculation or adsorption processes do not affect the flux of riverine DOC through the estuary. The DOC inputs from the Severn (1.7–2.7 × 10¹⁰ g Cyr^?1) and other rivers (2.6–3.4 × 10¹⁰ g Cyr^?1) are the principal sources of DOC in the estuary and correspond to an export of 0.7–1.1% of the terrestrial productivity from the river catchment to the ocean. This export rate is in accord with recent predictions derived from global compilations of organic inputs from rivers and would imply that the global flux of riverine DOC could be as high as 7.8 × 10¹⁴ g Cyr^?1 which is 5 times greater than some previous estimates.The geochemical significance of a conservative delivery of riverine DOC to the ocean is that irrespective of which flux estimate is considered, such river inputs would make a significant contribution (~SO%) to oceanic DOC, and that the steady-state oceanic DOC flux would have to be significantly greater than present estimates (2.9 × 10¹⁴ g Cyr^?1) which are based on a mean radio carbon age of 3400 yr.An alternative, more realistic DOC flux model, which assumes a polydisperse age distribution about the mean age, is shown to yield the higher oceanic DOC fluxes required. Flocculation and adsorption processes would remove less than 10% and 0.2% respectively of riverine DOC in estuaries.     

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d^?1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d^?1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20–75 μM; 0.26–1 mg L^?1) and ultraviolet absorption coefficient values (a ₂₅₄?<?5 m^?1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.     

Temporal variation and fluxes of dissolved and particulate organic carbon in the Apure,Caura and Orinoco rivers,Venezuela

The concentrations of total suspended sediments (TSS), dissolved organic carbon (DOC) and particulate organic carbon (POC) were measured in water samples taken monthly in the Apure, Caura and Orinoco rivers during a hydrological cycle (between Sept. 2007 and Aug. 2008). The DOC concentration values ranged between 1.5 and 6.8 mgC l⁻¹ in the Apure River; 2.07 and 4.9 mgC l⁻¹ in the Caura River and 1.66 and 5.35 mgC l⁻¹ in the Orinoco River. The mean concentration of DOC was 3.9 mgC l⁻¹ in the Apure River, 3.24 mgC l⁻¹ in the Caura River and 2.92 mgC l⁻¹ in the Orinoco River at Puerto Ordaz. The three rivers showed a similar temporal pattern in the concentrations of DOC, with higher DOC values during the increasing branch of the hydrograph due to wash-out processes of the organic material stored in soils. The mean concentration values of POC were 1.33 mgC l⁻¹; 0.77 mgC l⁻¹ and 0.91 mgC l⁻¹ in the Apure, Caura and Orinoco rivers, respectively. The inverse relationship found between the percentage in weight of the POC and the concentrations of TSS in the three rivers fits a logarithmic model, as it has been previously reported for other worldwide rivers. The POC concentrations in the Orinoco River showed a positive relationship with the TSS, suggesting that the POC in the Orinoco is the result of terrestrially organic matter. Although the fluxes of organic carbon (OC) in the three studied rivers are dependent on the values of water discharge, the fluxes of DOC during the increasing branch of the hydrograph are higher than those found during the decreasing stage, due to the yield of organic material accumulated in soils during the preceding dry season. The mean annual flux of total organic carbon (TOC) of the Orinoco River at Puerto Ordaz was about 4.27 × 10⁶ TonC yr⁻¹. Of this, 3.28 × 10⁶ TonC yr⁻¹ (77%) represents the flux of DOC and about 0.99 TonC yr⁻¹ (23%) represents the flux of POC. The mean annual input of TOC from the Apure River to the Orinoco River was about 4.92 × 10⁵ TonC yr⁻¹ (11.5%), while the contribution of TOC from the Caura River to the Orinoco River was estimated at 3.05 × 10⁵ TonC yr⁻¹ (7.1%).The values of annual transport of TOC calculated for the Apure, Caura and Orinoco rivers were lower than those reported twenty years ago. This could be related to interannual variations of precipitation in the Orinoco Basin, due to runoff variations can have a strong effect on the fluxes of OC from land to rivers.     

Some observations on the stable carbon isotope composition of dissolved and particulate organic carbon in the marine environment

δ¹³C_PDB compositions for 39 samples of dissolved organic carbon (DOC) from the Gulf of Mexico-Caribbean Sea-Atlantic Ocean system, the South Pacific and Ross Sea are reported. Deep water values are similar with a mean of ?21.8%. attesting to the homogeneity of the oceanic DOC pool. In Antarctic waters, a 5%. difference between DOC and particulate organic carbon (POC), with POC having values similar to modern plankton (δ¹³C_PDB approx ?27%.) supports the idea of the transient nature of POC as compared to DOC.Total, lipid, acid hydrolyzed, amino acid and residue fractions of POC are about 5, 3, 7, 5 and 3%. respectively, more negative in 2000 m water as compared to surface water samples from the Gulf of Mexico.     

Groundwater chemistry of Al under Dutch sandy soils: Effects of land use and depth

Aluminium has received great attention in the second half of the 20th century, mainly in the context of the acid rain problem mostly in forest soils. In this research the effect of land use and depth of the groundwater on Al, pH and DOC concentration in groundwater under Dutch sandy soils has been studied. Both pH and DOC concentration play a major role in the speciation of Al in solution. Furthermore, the equilibrium with mineral phases like gibbsite, amorphous Al(OH)₃ and imogolite, has been considered. Agricultural and natural land use were expected to have different effects on the pH and DOC concentration, which in turn could influence the total Al concentration and the speciation of Al in groundwater at different depths (phreatic, shallow and deep). An extensive dataset (n = 2181) from the national and some provincial monitoring networks on soil and groundwater quality was used. Land use type and groundwater depth did influence the pH, and Al and DOC concentrations in groundwater samples. The Al concentration ranged from <0.4 μmol L⁻¹ at pH > 7 to 1941 μmol L⁻¹ at pH < 4; highest Al concentrations were found for natural-phreatic groundwater. The DOC concentration decreased and the median pH increased with depth of the groundwater. Natural-phreatic groundwater showed lower pH than the agricultural-phreatic groundwater. Highest DOC concentrations were found for the agricultural-phreatic groundwater, induced by the application of organic fertilizers. Besides inorganic complexation, the NICA-Donnan model was used to calculate Al³⁺ concentrations for complexation with DOC. Below pH 4.5 groundwater samples were mainly in disequilibrium with a mineral phase. This disequilibrium is considered to be the result of kinetic constraints or equilibrium with organic matter. Log K values were derived by linear regression and were close to theoretical values for Al(OH)₃ minerals (e.g. gibbsite or amorphous Al(OH)₃), except for natural-phreatic groundwater for which lower log K values were found. Complexation of Al with DOC is shown to be an important factor for the Al concentrations, especially at high DOC concentrations as was found for agricultural-phreatic groundwater.     

Isotope Constraints on the Aquatic Carbon Budget: Langat Watershed,Malaysia

Langat River drains a tropical watershed in the southwest of the Malaysian Peninsula. The watershed is heavily urbanized in its downstream portion. Water samples were collected from May 2010 to December 2011, at three localities along the main stem river, 1 location at its Semenyih tributary and from an upstream groundwater source. Concentration and δ¹³C data of riverine DIC and DOC indicate the dominance of C3 plant-derived material as the primary source of carbon, with δ¹³C_DIC values enriched in ¹³C relative to that of the C3 source. This enrichment is likely due to CO₂ outgassing, as calculated concentrations of riverine CO₂ are significantly higher than ambient atmospheric values, with methanogenic activity a theoretically possible contributing factor, particularly at the upstream location. The Langat River therefore acts as a net source of CO₂, with a total sub-basin flux of 19.7 × 10³ t C year^?1. This is comparable to the sum of riverine DOC, DIC and POC loss rates from the sub-basin, calculated as 24.5 × 10³ t C year^?1, and highlights the significance of CO₂ evasion from water bodies to the atmosphere for balancing the budget of the terrestrial carbon cycle. The DIC and DOC concentration and δ¹³C data also suggests that in the more urbanized downriver areas, much of the organic carbon input may be anthropogenicaly derived due to ubiquity of sewage treatment plants and landfill sites. Such human-induced perturbations to riverine carbon cycling should be taken into account in future studies of urbanized watersheds.     

Seasonal Dynamics in Dissolved Organic Carbon Concentrations in a Coastal Water-Table Aquifer at the Forest-Marsh Interface

The seasonal dynamics of dissolved organic carbon (DOC) in a subterranean estuary were examined in a coastal water-table aquifer extending across a forest-marsh interface into an adjacent tidal creek that leads to North Inlet (SC). The aquifer is characterized by groundwater flow from the forest recharge area towards the creek. DOC concentrations range from 50 to 140 mg L^-1 in the shallow portions of the aquifer below the forest and undergo seasonal changes that are inversely related to temperature and precipitation conditions. Markedly lower DOC concentrations (<10 mg L^-1) in the deep portion of the aquifer are consistent with the loss of a large fraction of the original DOC along the groundwater flow paths. Mass balance estimates indicate that over 60% of the DOC losses are due to sorption reactions whereas the rest appear to be caused by heterotrophic decay. Groundwater DOC discharge from the forest, which occurs in a restricted zone of the high marsh, is 5.5 mg carbon m^-2 d^-1 and accounts for a minor component of the annual carbon export from North Inlet. In contrast, moderately saline (2–12 ppt) ground waters below the marsh display elevated DOC concentrations (20 mg L^-1) that appear to be the result of mixing of fresh ground waters and surface seawater during tidal seepage and concentration during evapotranspiration. The flux of DOC associated with the discharge of these saline ground waters is 600 mg carbon m^-2 d^-1, which represents a significant fraction of the annual DOC budget for North Inlet.     

Landscape scale controls on the vascular plant component of dissolved organic carbon across a freshwater delta

Lignin phenol concentrations and compositions were determined on dissolved organic carbon (DOC) extracts (XAD resins) within the Sacramento-San Joaquin River Delta (the Delta), the tidal freshwater portion of the San Francisco Bay Estuary, located in central California, USA. Fourteen stations were sampled, including the following habitats and land-use types: wetland, riverine, channelized waterway, open water, and island drains. Stations were sampled approximately seasonally from December, 1999 through May, 2001. DOC concentrations ranged from 1.3 mg L⁻¹ within the Sacramento River to 39.9 mg L⁻¹ at the outfall from an island drain (median 3.0 mg L⁻¹), while lignin concentrations ranged from 3.0 μg L⁻¹ within the Sacramento River to 111 μg L⁻¹ at the outfall from an island drain (median 11.6 μg L⁻¹). Both DOC and lignin concentrations varied significantly among habitat/land-use types and among sampling stations. Carbon-normalized lignin yields ranged from 0.07 mg (100 mg OC)⁻¹ at an island drain to 0.84 mg (100 mg OC)⁻¹ for a wetland (median 0.36 mg (100 mg OC)⁻¹), and also varied significantly among habitat/land-use types. A simple mass balance model indicated that the Delta acted as a source of lignin during late autumn through spring (10-83% increase) and a sink for lignin during summer and autumn (13-39% decrease). Endmember mixing models using S:V and C:V signatures of landscape scale features indicated strong temporal variation in sources of DOC export from the Delta, with riverine source signatures responsible for 50% of DOC in summer and winter, wetland signatures responsible for 40% of DOC in summer, winter, and late autumn, and island drains responsible for 40% of exported DOC in late autumn. A significant negative correlation was observed between carbon-normalized lignin yields and DOC bioavailability in two of the 14 sampling stations. This study is, to our knowledge, the first to describe organic vascular plant DOC sources at the level of localized landscape features, and is also the first to indicate a significant negative correlation between lignin and DOC bioavailability within environmental samples. Based upon observed trends: (1) Delta features exhibit significant spatial variability in organic chemical composition, and (2) localized Delta features appear to exert strong controls on terrigenous DOC as it passes through the Delta and is exported into the Pacific Ocean.     

Geochemical characteristics and organic carbon sources within the upper reaches of the Xi River,southwest China during high flow

Carbon (POC, DOC) and carbon isotopes (δ¹³C) within two headwater tributaries to the Xi River Basin, southwest China were analyzed to document the geochemical characteristics and sources of organic carbon (C) within basins characterized by a monsoonal climate and karst landforms. δ¹³ C _POC value and C/N ratio data indicate that suspended soil organic carbon (SOC) was an important source of POC in both the Nanpan and Beipan rivers (i.e., the studied tributaries). However, differences in C sources exist between the Nanpan and Beipan River Basins. Higher terrestrial plants supplied a portion of the POC within the Beipan River. In contrast, the Nanpan River was characterized by an inverse correlation between POC and DOC, and a positive relationship between the δ¹³C values. These trends indicate that DOC within the Nanpan River was partly derived from the degradation of soil C within the water column. In addition, the interception of C by hydrological projects (e.g., dams) positioned along the Nanpan River led to higher DOC/POC ratios. In contrast, within the Beipan River δ¹³C _DOC values range from ?20 to ?25.2 ‰ and are consistent with ratios associated with soil C, suggesting that leaching of C from catchment soil was the dominant source of DOC. Organic C in tributaries to the Beipan River may also have been derived from intense upland soil erosion, a process that resulted in the lowest DOC/POC ratios. The collected data indicate that land-use changes have potentially influenced regional- to local-scale organic C budgets within subtropical basins subjected to karstification.     

Chemistry and transport of soluble humic substances in forested watersheds of the Adirondack Park,New York

Studies were conducted in conjunction with the Integrated Lake-Watershed Acidification Study (ILWAS) to examine the chemistry and leaching patterns of soluble humic substances in forested watersheds of the Adirondack region. During the summer growing season, mean dissolved organic carbon (DOC) concentrations in the ILWAS watersheds ranged from 21–32 mg C l^?1 in O/A horizon leachates, from 5–7 mg C l^?1 in B horizon leachates, from 2–4 mg C l^?1 in groundwater solutions, from 6–8 mg C l^?1 in first order streams, from 3–8 mg C l^?1 in lake inlets, and from 2–7 mg C l^?1 in lake outlets. During the winter, mean DOC concentrations dropped significantly in the upper soil profile. Soil solutions from mixed and coniferous stands contained as much as twice the DOC concentration of lysimeter samples from hardwood stands. Results of DOC fractionation analysis showed that hydrophobia and hydrophilic acids dominate the organic solute composition of natural waters in these watersheds. Charge balance and titration results indicated that the general acid-base characteristics of the dissolved humic mixture in these natural waters can be accounted for by a model organic acid having an average_pK_a of 3.85, an average charge density of 4–5 μeq mg^?1 C at ambient pH, and a total of 6–7 meq COOH per gram carbon.     

DOC dynamics in a small temperate estuary: Simultaneous addition and removal processes and implications on observed nonconservative behavior

Dissolved organic carbon (DOC) dynamics in the Pawcatuck River estuary, a small temperate estuary in Rhode Island, United States, were examined through the use of field transect and in situ production studies. In late summer, when river discharge was minimal, phytoplankton blooms occurred in the upper reaches of the estuary and released large amounts of autochthonous DOC that accumulated in the middle reaches of the estuary. DOC production rates in August months, calculated both by mixing diagrams and in situ DOC incubations, ranged from 6.67 to 34.7 μmol C l⁻¹ d⁻¹ and were positively correlated with DCMU-enhanced fluorescence, an estimate of phytoplankton photosynthetic activity (r²=0.796, p<0.001). The percent extracellular release (PER) of DOC from phytoplankton, calculated from measured in situ DOC production and net phytoplankton production (NPP) rates, ranged from 5.8% to 40.6% and was negatively correlated with NPP (r²=0.80, p<0.01). Accumulated DOC was principally nonhumic in nature, and the humic DOC component behaved quite differently with either conservative mixing or significant removal at the head of the estuary. Humic removal at times amounted to approximately 50% of the humic material and 25% of the total incoming riverine DOC. These large humic losses were not observed in bulk DOC-salinity mixing diagrams but required distinct analyses of the humic and nonhumic components. DOC addition and removal processes co-occur in this system and observation of bulk DOC mixing diagrams may mask the true dynamic nature of the estuarine DOC pool. The net result of the DOC addition and removal processes is a seasonally variable transformation of a humic-rich incoming riverine DOC to a nonhumic enriched bulk DOC component that varies seasonally and with river discharge.     

Sources of dissolved organic carbon in forest soils: evidences from the differences of organic carbon concentration and isotope composition studies

There is considerable discussion and uncertainty in the literature regarding the importance of fresh litter versus older soil organic matter as sources of soil dissolved organic carbon (DOC) in forest floor. In this study, the differences of organic carbon concentration and stable isotope composition were analyzed under different background conditions to identify the origins of DOC in forest soil. The data show that there is no significant difference in SOC content between these collected soil samples (P > 0.05), but the litter-rich surface soils have relatively higher DOC concentration than the litter-lacking (P < 0.01) ones, and the δ ¹³C values of DOC (δ ¹³C_DOC) are closer to δ ¹³C of litter than δ ¹³C values of SOC (δ ¹³C_SOC). In the litter-lacking surface soil samples, the range of δ ¹³C_DOC is between δ ¹³C_SOC and δ ¹³C of dominant plant leaves. These results suggest that DOC mainly derive from litter in the litter-rich surface soil with, and the main path of DOC sources may change with surrounding conditions. In addition, δ ¹³C_SOC and δ ¹³C_DOC become more positive, and the absolute values of Δ (δ ¹³C_DOC − δ ¹³C_SOC) decrease with depth in the soil profiles, which indicate that the percentage of DOC below 5 cm, derived from degradation of humus, may increase with soil depth.     

Fractionation of dissolved organic matter affected by polyvalent metal cations

The purpose of the study was to evaluate the influence of polyvalent cations known to form complexes with natural organic substances on the operational fractionation of dissolved organic matter (DOM) using XAD-8 adsorber resin. Dissolved organic matter solutions from a forest floor were treated with increasing concentrations of polyvalent metal cations (Ca²⁺, Al³⁺, Fe³⁺) at different pH levels. Then the concentrations of total dissolved organic carbon (DOC) and the distribution between hydrophilic and hydrophobic DOC were determined. The concentrations of total DOC decreased slightly when the C/metal ratio was less than 10, especially for Al and Fe. Hydrophilic DOC increased and hydrophobic DOC decreased with increasing concentrations of metal cations. Effects increased in the order Ca<Al<Fe and were more pronounced at low DOC concentrations and high pH values. The reason for the reduction of the DOC concentrations seemed to be the formation of insoluble metal–DOM complexes, while soluble metal–DOM complexes may induce an alteration of the distribution between hydrophilic and hydrophobic DOC. Thus, the polyvalent cations and their concentration need to be considered when DOM fraction distributions, determined with XAD-8 resin, of different waters are compared, especially at low DOC contents and high pH.     

Stability of Titanium Dioxide Nanoparticle Agglomerates in Transitional Waters and Their Effects Towards Plankton from Lagoon of Venice (Italy)

The present study explores the effect of salinity and dissolved organic carbon (DOC) gradients on the stability and reactivity of titanium dioxide nanoparticle (TiO₂-NP) agglomerates in ambient water from the Lagoon of Venice and their possible effect on nauplii sampled at the same locations. In all ambient water samples, TiO₂-NPs formed rapidly micrometre-sized agglomerates. The increase in the salinity and concomitant decrease in DOC content induced the formation of larger agglomerates, with z-average hydrodynamic diameter increasing with TiO₂-NP concentration and exposure duration. Under the studied conditions, ζ-potential exhibited negative values. In line with agglomeration results, enhancement of the salinity and lower DOC resulted in less negative ζ-potential with close to 0 values in the dispersions of 100 mg L^?1 TiO₂-NPs in sea water. Two-hour exposure to micrometre-sized agglomerates of TiO₂-NPs resulted in an increase in the fluorescence of propidium iodide (PI) stained nauplii in comparison with unexposed controls, but had no effect at 24-h exposure. The increase in nauplii-associated PI fluorescence was more noticeable in dispersions containing 100 mg L^?1 than those containing 10 mg L^?1 TiO₂-NPs, suggesting membrane permeability alteration in a concentration-dependent manner. However, the PI staining results have to be interpreted with caution because of the possible dye binding to the nauplii surface without penetration of cellular membrane. The effect of TiO₂-NPs on nauplii was more pronounced at higher salinity and decreased with increasing DOC concentrations at 2 h, while no trends were found at 24-h exposure, as well as exposure to 100 mg L^?1 TiO₂-NPs.     

Mobilization of arsenic from acid deposition – The Elbe River catchment,Czech Republic

Temporal changes of As concentration in surface waters were observed in some areas of the Czech Republic. Mobilized As originates from past atmospheric deposition. To understand the factors influencing As aqueous concentration and mobility the chemistry and runoff generation of a number of brooks, springs and rivers in the central part of the Elbe River catchment, Czech Republic, were monitored. Seasonal variations of As (from 0.5 to 10.5 μg L⁻¹), Fe (from 0.05 to 3.9 mg L⁻¹) and DOC (dissolved organic C – from 1.2 to 17.5 mg L⁻¹) were observed in monitored stream waters with maximum values of As and Fe in the summer months at pH values 7.6–7.8. The concentration of As in particles with a diameter < 60 μm correlates with the Fe concentration. There is no correlation between Fe and As in filtered samples (<0.45 μm). The As concentration in stream water colloids depends on an increase in DOC concentration and a decrease in ionic strength. The DOC stabilizes As in solution and reduces its re-adsorption on Fe colloids and consequently As concentration in the stream increases.     

The distribution and stable carbon isotopic composition of dissolved organic carbon in estuaries

The distributions of dissolved organic carbon (DOC) and the natural carbon isotope ratio of DOC (DO¹³C) in estuaries reflect the predominant sources and sinks of organic matter from both allochthonous and autochthonous origins. The traditional view is that DOC in land-margin ecosystems reflects mainly the mixing of land-derived and oceanic DOC. However, this view is not consistent with the bulk of our data from a survey of DOC and DO¹³C distributions in estuaries on the East and Gulf coasts of the USA. While it is accurate that the DOC in estuaries includes material derived from land and from the ocean, the distributions of DOC and DO¹³C in several estuaries reflect additional DOC inputs from estuarine phytoplankton and tidal marshes. Even when DOC concentrations were distributed conservatively, the isotopic composition of the DOC revealed the existence of a dynamic cycle of DOC input and removal in some systems.